UY31232A1 - COMPOUNDS DERIVED FROM DIBENZOTIFENILAMINO-CROMEN-4-ACTIVE WAVES REPLACED AND ITS ISOMERS AND APPLICATIONS - Google Patents
COMPOUNDS DERIVED FROM DIBENZOTIFENILAMINO-CROMEN-4-ACTIVE WAVES REPLACED AND ITS ISOMERS AND APPLICATIONSInfo
- Publication number
- UY31232A1 UY31232A1 UY31232A UY31232A UY31232A1 UY 31232 A1 UY31232 A1 UY 31232A1 UY 31232 A UY31232 A UY 31232A UY 31232 A UY31232 A UY 31232A UY 31232 A1 UY31232 A1 UY 31232A1
- Authority
- UY
- Uruguay
- Prior art keywords
- group
- dibenzotifenilamino
- cromen
- isomers
- replaced
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Urology & Nephrology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurology (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Gastroenterology & Hepatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Un compuestos de la formula I, en donde: R1 y R2 se seleccionan de manera independiente entre hidrogeno, un grupo alquilo C1-7, un grupo heterociclilo C3-20 o arilo C5-20 opcionalmente sustituido, o juntos pueden formar, junto con el átomo de nitrogeno al cual están unidos, un anillo heterocíclico opcionalemente sustituido que tiene entre 4 y 8 átomos de anillo; X es CH o N; n es 1 o 2; RC1 y Rc2 se seleccionan de manera independiente entre H y metilo; cuando X es N, Rx se selecciona del grupo que consiste de H, y un grupo opcionalmente sustituido de alquilo C1-7, heterociclilo C3-20, arilo C5-20, acilo, éster, amido y sulfonilo; y cuando X es CH, Rx se selecciona del grupo que consiste de H, y un grupo opcionalmente sustituido de alquilo C1-7, heterociclilo C3-20, arilo C5-20, acilo, éster, amido, sulfonilo, amino y éter.A compound of the formula I, wherein: R1 and R2 are independently selected from hydrogen, a C1-7 alkyl group, an optionally substituted C3-20 heterocyclyl or C5-20 aryl group, or together they can form, together with the nitrogen atom to which they are attached, an optionally substituted heterocyclic ring having between 4 and 8 ring atoms; X is CH or N; n is 1 or 2; RC1 and Rc2 are independently selected from H and methyl; when X is N, Rx is selected from the group consisting of H, and an optionally substituted group of C1-7 alkyl, C3-20 heterocyclyl, C5-20 aryl, acyl, ester, amido and sulfonyl; and when X is CH, Rx is selected from the group consisting of H, and an optionally substituted group of C1-7 alkyl, C3-20 heterocyclyl, C5-20 aryl, acyl, ester, amido, sulfonyl, amino and ether.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US95063107P | 2007-07-19 | 2007-07-19 | |
US3656008P | 2008-03-14 | 2008-03-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY31232A1 true UY31232A1 (en) | 2009-03-02 |
Family
ID=39791057
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY31232A UY31232A1 (en) | 2007-07-19 | 2008-07-17 | COMPOUNDS DERIVED FROM DIBENZOTIFENILAMINO-CROMEN-4-ACTIVE WAVES REPLACED AND ITS ISOMERS AND APPLICATIONS |
Country Status (14)
Country | Link |
---|---|
US (1) | US20090042865A1 (en) |
EP (1) | EP2176254A1 (en) |
JP (1) | JP2010533694A (en) |
KR (1) | KR20100063701A (en) |
CN (1) | CN101754964A (en) |
AR (1) | AR067613A1 (en) |
AU (1) | AU2008277418A1 (en) |
BR (1) | BRPI0814797A2 (en) |
CA (1) | CA2693926A1 (en) |
CL (1) | CL2008002130A1 (en) |
RU (1) | RU2009149210A (en) |
TW (1) | TW200918528A (en) |
UY (1) | UY31232A1 (en) |
WO (1) | WO2009010761A1 (en) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0119865D0 (en) * | 2001-08-14 | 2001-10-10 | Cancer Res Campaign Tech | DNA-PK inhibitors |
GB2420781B (en) * | 2003-08-13 | 2008-07-09 | Kudos Pharm Ltd | Aminopyrones and their use as ATM inhibitors |
BRPI0515498A (en) * | 2004-09-20 | 2008-07-29 | Kudos Pharm Ltd | dna-pk inhibitors |
WO2006085067A1 (en) * | 2005-02-09 | 2006-08-17 | Kudos Pharmaceuticals Limited | Atm inhibitors |
AR054438A1 (en) * | 2005-04-15 | 2007-06-27 | Kudos Pharm Ltd | DNA INHIBITORS -PK |
US7638541B2 (en) | 2006-12-28 | 2009-12-29 | Metabolex Inc. | 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine |
KR20100033419A (en) | 2007-07-19 | 2010-03-29 | 메타볼렉스, 인코포레이티드 | N-azacyclic substituted pyrrole, pyrazole, imidazole, triazole and tetrazole derivatives as agonists of the rup3 or gpr119 receptor for the treatment of diabetes and metabolic disorders |
JP5909185B2 (en) | 2009-10-01 | 2016-04-26 | シマベイ セラピューティクス, インコーポレーテッド | Substituted tetrazol-1-ylphenoxymethylthiazol-2-ylpiperidinylpyrimidine salt |
WO2011137428A1 (en) * | 2010-04-30 | 2011-11-03 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Methods of treating hiv infection: inhibition of dna dependent protein kinase |
CA2802541A1 (en) | 2010-06-23 | 2011-12-29 | Metabolex, Inc. | Compositions of 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine |
RS61664B1 (en) | 2012-04-24 | 2021-04-29 | Vertex Pharma | Dna-pk inhibitors |
RS58374B1 (en) | 2013-03-12 | 2019-03-29 | Vertex Pharma | Dna-pk inhibitors |
CN104892589A (en) | 2014-03-07 | 2015-09-09 | 中国科学院上海药物研究所 | Heterocyclic compound, preparation method therefor and use thereof |
CN109862896A (en) | 2016-08-03 | 2019-06-07 | 西玛贝医药公司 | For treating the Oxymethylene aryl compound of inflammatory gastrointestinal disease or gastrointestinal disorder |
TW201815418A (en) | 2016-09-27 | 2018-05-01 | Vertex Pharma | Method for treating cancer using a combination of DNA-damaging agents and DNA-PK inhibitors |
CN111053903A (en) * | 2019-12-26 | 2020-04-24 | 深圳市纳诺艾医疗科技有限公司 | Application of compound of nucleic acid analogue carrying resonance atom |
TW202235074A (en) * | 2021-01-05 | 2022-09-16 | 大陸商山東軒竹醫藥科技有限公司 | polycyclic kinase inhibitor |
Family Cites Families (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0753725B2 (en) * | 1987-10-08 | 1995-06-07 | 富山化学工業株式会社 | 4H-1-benzopyran-4-one derivative and its salt, their production method and anti-inflammatory agent containing them |
US5284856A (en) * | 1988-10-28 | 1994-02-08 | Hoechst Aktiengesellschaft | Oncogene-encoded kinases inhibition using 4-H-1-benzopyran-4-one derivatives |
US5703075A (en) * | 1988-12-21 | 1997-12-30 | Pharmacia & Upjohn Company | Antiatherosclerotic and antithrombotic 1-benzopyran-4-ones and 2-amino-1,3-benzoxazine-4-ones |
US5252735A (en) * | 1990-06-29 | 1993-10-12 | The Upjohn Company | Antiatherosclerotic and antithrombotic 2-amino-6-phenyl-4H-pyran-4-ones |
US5302613A (en) * | 1990-06-29 | 1994-04-12 | The Upjohn Company | Antiatheroscleroic and antithrombotic 2-amino-6-phenyl-4H-pyran-4-ones |
US5922755A (en) * | 1993-04-09 | 1999-07-13 | Toyama Chemical Co., Ltd. | Immunomodulator, cell adhesion inhibtor, and agent for treating, and preventing autoimmune diseases |
US5733920A (en) * | 1995-10-31 | 1998-03-31 | Mitotix, Inc. | Inhibitors of cyclin dependent kinases |
JP4103968B2 (en) * | 1996-09-18 | 2008-06-18 | 株式会社半導体エネルギー研究所 | Insulated gate type semiconductor device |
US6348311B1 (en) * | 1999-02-10 | 2002-02-19 | St. Jude Childre's Research Hospital | ATM kinase modulation for screening and therapies |
US6387640B1 (en) * | 1999-02-10 | 2002-05-14 | St. Jude Children's Research Hospital | ATM kinase modulation for screening and therapies |
US6333180B1 (en) * | 1999-12-21 | 2001-12-25 | International Flavors & Fragrances Inc. | Bioprocess for the high-yield production of food flavor-acceptable jasmonic acid and methyl jasmonate |
JP2004501191A (en) * | 2000-06-28 | 2004-01-15 | テバ ファーマシューティカル インダストリーズ リミティド | Carvedilol |
GB0119863D0 (en) * | 2001-08-14 | 2001-10-10 | Cancer Res Campaign Tech | DNA-PK inhibitors |
GB0119865D0 (en) * | 2001-08-14 | 2001-10-10 | Cancer Res Campaign Tech | DNA-PK inhibitors |
US7049313B2 (en) * | 2002-02-25 | 2006-05-23 | Kudos Pharmaceuticals Ltd. | ATM inhibitors |
AU2003229953A1 (en) * | 2002-04-30 | 2003-11-17 | Kudos Pharmaceuticals Limited | Phthalazinone derivatives |
GB2420781B (en) * | 2003-08-13 | 2008-07-09 | Kudos Pharm Ltd | Aminopyrones and their use as ATM inhibitors |
BRPI0515498A (en) * | 2004-09-20 | 2008-07-29 | Kudos Pharm Ltd | dna-pk inhibitors |
WO2006085067A1 (en) * | 2005-02-09 | 2006-08-17 | Kudos Pharmaceuticals Limited | Atm inhibitors |
AR054438A1 (en) * | 2005-04-15 | 2007-06-27 | Kudos Pharm Ltd | DNA INHIBITORS -PK |
JP5781720B2 (en) * | 2008-12-15 | 2015-09-24 | ルネサスエレクトロニクス株式会社 | Semiconductor device and manufacturing method of semiconductor device |
-
2008
- 2008-07-17 UY UY31232A patent/UY31232A1/en not_active Application Discontinuation
- 2008-07-18 WO PCT/GB2008/002459 patent/WO2009010761A1/en active Application Filing
- 2008-07-18 BR BRPI0814797-3A2A patent/BRPI0814797A2/en not_active Application Discontinuation
- 2008-07-18 US US12/175,542 patent/US20090042865A1/en not_active Abandoned
- 2008-07-18 CN CN200880024849A patent/CN101754964A/en active Pending
- 2008-07-18 AU AU2008277418A patent/AU2008277418A1/en not_active Abandoned
- 2008-07-18 CA CA2693926A patent/CA2693926A1/en not_active Abandoned
- 2008-07-18 AR ARP080103124A patent/AR067613A1/en unknown
- 2008-07-18 TW TW097127524A patent/TW200918528A/en unknown
- 2008-07-18 KR KR1020107003763A patent/KR20100063701A/en not_active Application Discontinuation
- 2008-07-18 CL CL2008002130A patent/CL2008002130A1/en unknown
- 2008-07-18 JP JP2010516580A patent/JP2010533694A/en not_active Withdrawn
- 2008-07-18 EP EP08775986A patent/EP2176254A1/en not_active Withdrawn
- 2008-07-18 RU RU2009149210/04A patent/RU2009149210A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CN101754964A (en) | 2010-06-23 |
AR067613A1 (en) | 2009-10-14 |
US20090042865A1 (en) | 2009-02-12 |
KR20100063701A (en) | 2010-06-11 |
CA2693926A1 (en) | 2009-01-22 |
CL2008002130A1 (en) | 2009-01-02 |
EP2176254A1 (en) | 2010-04-21 |
TW200918528A (en) | 2009-05-01 |
JP2010533694A (en) | 2010-10-28 |
RU2009149210A (en) | 2011-08-27 |
AU2008277418A1 (en) | 2009-01-22 |
BRPI0814797A2 (en) | 2015-02-03 |
WO2009010761A1 (en) | 2009-01-22 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
109 | Application deemed to be withdrawn |
Effective date: 20171009 |